A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4692n54



Internal ID20138116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85235254..85600273hg38UCSC Ensembl
chr15:85778485..86143504hg19UCSC Ensembl
chr15:83579489..83944508hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38365020
hg19365020
hg18365020
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570299, nsv570302, nsv570300, nsv570297, nsv570295, nsv570301, nsv570304, nsv570303
Samples1798860114_A, 1782681216_A
Known GenesAKAP13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4692n54
Frequency
Sample Size17421
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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